The present invention relates to room temperature or thermally polymerizable/curable episulfide based compositions for making polymerized/cured episulfide based resins, and in particular episulfide based compositions which can be fastly polymerized/cured, as well as to a room temperature or thermal polymerization process for making such episulfide based resins.
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1. Polymerizable composition for making episulfide based resins comprising:
A) at least one episulfide compound bearing at least one episulfide and at least one functional group capable of polymerizing with episulfide groups, and
B) an effective amount of a polymerization catalyst system comprising:
at least one salt of formula
Mmp+Yn− wherein
Mp+ is a cation selected from the group consisting of alkaline metals, alkaline earth metals, transitions metals and ammonium groups of formula NR+4 in which R is an alkyl radical,
Y− is an anion such as the corresponding acid YH has a pka fulfilling the condition 0.5≦pKa≦14 with the proviso that when Mp+is an ammonium group, the catalyst system further comprises an electro-donor compound,
P is the valency of the cation,
n=m×p, and
at least one tertiary amine.
2. Polymerizable composition according to
3. Polymerizable composition according to
4. Polymerizable composition according to
5. Polymerizable composition according to
6. Polymerizable composition according to
7. Polymerizable composition according to
8. Polymerizable composition according to
(R)3N in which the R groups represent, independently from each other, an alkyl radical, a cycloalkyl radical or mixtures thereof.
9. Polymerizable composition according to
10. Polymerizable composition according to
11. Polymerizable composition according to
12. Polymerizable composition according to
13. Composition according to
14. Composition according to
wherein X1 represents O, S or NH, x1 is an integer from 3 to 6,
X2, X3 and X4 represent O or S,
n2, n3, n4, y2, y3, y4 are 2 or 3, and
x2, x3, x4 are 2 or 3.
15. Composition according to
16. The composition of
in which R1 represents a hydrocarbon group having 1 to 10 carbon atoms, R2, R3 and R4 each represents an hydrogen atom or a hydrocarbon group having 1 to 10 carbon atoms, X represents S or O with the provisio that in the molecule the average number of S represented by X is about 50% of the total number of S and O constituting the three membered ring.
17. Composition of
in which R5, R6, R7, R8, R9 and R10 each represents an hydrogen atom or a hydrocarbon group having 1 to 10 carbon atoms, X represents S or O with the proviso that, in the molecule, the average number of S represented by X is about 50% or more of the total number of S and O constituting the three member rings, m represents an integer from 0 to 6 and n represents an integer from 0 to 4.
18. The composition of
19. The composition of
20. The composition according to
R′(SH)n′ in which n′ is an integer from 2 to 6 and R′ is an organic group of valency equal to n′.
21. The composition according to
22. Composition according to
23. Composition according to
wherein:
R11 is independently H or C1-C5 alkyl group,
R12 is H, an halogen, or a C1-C5 alkyl group,
Z is —N═C═O or —N═C═S;
a is an integer ranging from 1 to 4, b is an integer ranging from 2 to 4 and a+b≦6; and
x is an integer from 1 to 10.
24. Composition according to
25. Composition according to
26. Process for making a cast episulfide based resin article comprising:
preparing a composition as set forth in
filling a mold with the prepared composition;
heating the filled mold at a first temperature of 50° C. or less up to the obtention of a gel;
thereafter, heating at a second temperature higher than the first temperature up to the obtention of a hard resin; and
removing the cast article from the mold.
27. The process according to
28. The process according to
29. The process according to
30. The process according to
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(1) Field of the Invention
The present invention relates to room temperature or thermally polymerizable/curable episulfide based compositions for making polymerized/cured episulfide based resins, and in particular episulfide based compositions which can be fastly polymerized/cured, as well as to a room temperature or thermal polymerization process for making such episulfide based resins.
The polymerizable compositions and the polymerization process of the invention are particularly useful for making optical articles such as lenses, prisms, optical fibers, filters or for making different types of substrates, such as information recording substrates.
The polymerizable compositions and the polymerization process of the invention are also specifically suited for making various coatings and in particular coatings for optical applications.
(2) Description of the Prior Art
Plastic materials are widely used in the optical field and particularly in the ophthalmic field for their lightness, high impact resistance and tintable capability by immersion in a bath containing an organic dye.
Optically transparent plastic materials having a high refractive index nD=1.6 or even higher have been developped recently which renders it possible to manufacture optical articles such as lenses of lower thickness for an equivalent corrective power (optical power).
A class of such materials is comprised of episulfide based resins.
Document U.S. Pat. No. 5,807,975 discloses thermal polymerization and curing of diepisulfides, in particular for the manufacture of optical materials such as a lens material for spectacles. This thermal polymerization/curing of diepisulfides lasts for several hours, generally about 20 hours.
Episulfide compounds and their polymerization process are disclosed in EP-A-761.665 and EP-A-785.194.
Unfortunately, the polymerization of these polymerizable compositions needs a long thermal cycle, generally between 8 hours to several days in order to obtain fully polymerized articles without striation or strain.
Others have disclosed thermal or room temperature polymerization of episulfide compounds using, as catalyst, a salt of formula:
Mmp+Yn−
in which Mp+ is a cation selected from the group consisting of alkaline metals, alkaline earth metals, transition metals and ammonium groups, Y− is an anion of an acid fulfilling the condition 0.5≦Pka≦14, p is the valency of the cation and n=m×p. A preferred catalyst is KSCN.
Although the polymerization time is very significantly decreased when using such a salt catalyst, there is still a requirement to speed up the polymerization of any kind of episulfides without inducing striation and yellowness or without giving a run-away reaction.
Thus, the aim of the present invention is to provide polymerizable compositions for making episulfide based resins which are thermally polymerizable or polymerizable at room temperature in a short time, typically in less than 6 hours.
The invention also concerns a polymerization process, in particular a room temperature or thermal polymerization process, for making episulfide based resins which necessitates shorter cure time than the prior art processes.
The invention further concerns optical articles such as lenses made of the episulfide base resins resulting from the polymerization of the polymerizable compositions.
It has now been discovered that, by using an effective amount of a catalyst system comprising at least one salt of a specific class of salts and at least one tertiary amine in polymerizable compositions for making episulfide base resins, it was possible to use very short polymerization cycles, typically less than 6 hours, while still obtaining a polymerized resin which is optically transparent and free of striations and having good mechanical, scratch and heat resistance properties.
According to the present invention, there is provided thermally or room temperature polymerizable compositions for making episulfide base resins comprising:
Mp+ is a cation selected from the group consisting of alkaline metals, alkaline earth metals, transitions metals and ammonium groups of formula NR+4 in which R is an alkyl radical,
Y− is an anion such as the corresponding acid YH has a pKa fulfilling the condition 0.5≦pKa≦14 with the proviso than when Mp+ is an ammonium group, the catalyst system further comprises an electro-donor compound,
p is the valency of the cation,
n=m×p, and
at least one tertiary amine.
The preferred metallic cation of the salts of the catalyst system according to the invention are Li+, Na+, K+, Rb+, Mg2+, Ca2+ and Al3+. The particularly preferred metallic cations are Li+, Na+ and K+ due to their absence of colour and good solubility in the composition. Transition metals are less preferred because the salts thereof lead to coloured compositions and therefore coloured polymerized resins.
The preferred NR+4 groups are those in which R is a C1-C8 alkyl radical and more preferably, a methyl, ethyl, propyl, butyl or hexyl radical.
Preferably, Y− is an anion such as the corresponding acid YH which fulfils the conditions 0.5≦pKa≦10 and more preferably 0.5≦pKa≦8.
Preferably, the anion Y− is selected from the group consisting of thiocyanate, carboxylate, thiocarboxylate, acetylacetonate, diketone, acetoacetic ester, malonic ester, cyanoacetic ester, ketonitrile and anions of formula RS− wherein R is a substituted or non substituted alkyl group or phenyl group.
Preferably, the alkyl group is a C1-C6 alkyl group, such as methyl, ethyl and propyl.
The preferred anions Y− are SCN−, acetylacetonate, acetate, thioacetate, formate and benzoate.
The most preferred salt is KSCN.
Generally, the salt will be present in amounts ranging, based on the total weight of the polymerizable monomers present in the composition, from 0.001 to 2,5%, preferably 0.001 to 1%.
The tertiary amines of the catalyst system according to the invention may be represented by the formula:
(R)3N (I)
in which the R groups represent, independently from each other, an alkyl radical, generally a C1-C6 alkyl radical such as methyl, ethyl and propyl, preferably methyl, a cycloalkyl radical, generally a C5-C10 cycloalkyl radical such as cyclopentyl, cyclohexyl and cycloheptyl, preferably cyclohexyl, or mixtures thereof.
Among the preferred tertiary amines, there may be cited N,N-dimethylcyclohexylamine and N,N-dicyclohexylmethylamine.
Generally, the tertiary amine will be present in amounts ranging, based on the total weight of the polymerizable monomers present in the composition, from 0.5 to 5%, preferably from 0.05 to 2%.
In a preferred embodiment, the catalyst system according to the present invention further includes at least one electro-donor compound. The electro-donor compounds are preferably selected from the group consisting of acetonitrile compounds, amide compounds, sulfones, sulfoxides, trialkylphosphites, triarylphosphites, nitro compounds, ethyleneglycol ethers, crown ethers and kryptates.
Examples of acetonitrile compounds are:
##STR00001##
in which R is an alkyl group, preferably a C1-C6 alkyl group such as methyl, ethyl, propyl, butyl.
The amide compounds may be primary, secondary or tertiary amide compounds.
The triakylphosphites and triarylphosphites may be represented by formula: ##STR00002##
in which R, R′, R′″ are either an alkyl group, preferably a C1-C6 alkyl group or an aryl group such as a phenyl group. Preferred are trialkylphosphites, for example (C2H5O)3P.
Electro-donor compounds are preferably selected from crown ethers and kryptates.
These cyclic molecules are usually chosen to exhibit a good compromise between the heteroatom or metal size and the “cage” size, i.e. between the number of heteroatoms and the size of the cycle.
The preferred crownethers and kryptates may be represented by the following formulae: ##STR00003##
wherein X1 represents O, S or NH, x1 is an integer from 3 to 6, preferably from 3 to 4,
X2, X3 and X4 represent O or S, n2, n3, n4, y2, y3, y4 are 2 or 3, and x2, x3, x4 are 2 or 3.
Among the preferred crown ethers and kryptates there may be cited the following compounds: ##STR00004##
The electro-donor compounds are present, based on the total weight of the polymerizable monomers in amounts ranging from 0 to 5% by weight, preferably 0 to 1% by weight.
Preferred electro-donor compounds are crown-ethers, kryptates, trialkyl phosphites and aceto nitrile compounds, and most preferably crown-ethers such as 18-crown-6, 18-crown-7, 15-crown-5 and 15-crown-6.
The polymerizable compositions of the present invention may comprise a solvent for promoting the dissolution of the salt catalyst within the monomer.
Any polar organic solvent can be used such as acetonitrile, tetrahydrofurane or dioxane. However, to avoid bubble generation, it is preferred to use a reactive solvent containing a hydroxyl function. Suitable solvents are methanol, ethanol, acetone, acetonitrile, 3-methyl-2-butene-1 ol and 2-mercaptoethanol.
The amount of solvent is generally kept below 10% by weight, based on the total weight of the polymerizable monomers present, and is preferably about 5% by weight or less, to avoid haze and bubbling.
The polymerizable episulfide monomers of the invention have at least one episulfide functionality and preferably two or more episulfide functionalities per molecule.
The functional groups capable of polymerising with episulfide groups are epoxy, isocyanate, isothiocyanate, thiols, unsaturated c═c bonds such as acrylic, thioacrylic.
The most preferred episulfide monomers contain solely two episulfide functionalities and no other reactive functionality.
Preferably, the polymerizable monomers having at least one episulfide functionality are compounds having one or more episulfide structures represented by the following formula (IV) in one molecule: ##STR00005##
in which R1 represents a hydrocarbon group having 1 to 10 carbon atoms, R2, R3 and R4 each represents an hydrogen atom or a hydrocarbon group having 1 to 10 carbon atoms, X represents S or O with the provisio that in the molecule the average number of S represented by X is about 50% of the total number of S and O constituting the three membered ring.
A preferred class of polymerizable episulfide monomer is represented by compound of formula (V): ##STR00006##
in which R5, R6, R7, R8, R9 and R10 each represents an hydrogen atom or a hydrocarbon group having 1 to 10 carbon atoms, X represents S or O with the proviso that, in the molecule, the average number of S represented by X is about 50% or more of the total number of S and O constituting the three member rings, m represents an integer from 0 to 6 and n represents an integer from 0 to 4.
Preferably, R1 in formula (IV) represents a methylene group or ethylene group and R2, R3 and R4 in formula (IV) and R5, R6, R7, R8, R9 and R10 in formula (V) each preferably represents a hydrogen atom or a methyl group. It is more preferably that R1 represents a methylene group and R2, R3, R4, R5, R6; R7, R8, R9 and R10 each represents a hydrogen atom.
The average number of S in each of formula (IV) and formula (V) is 50% or more, preferably 90% or more, more preferably 95% or more and more preferably substantially 100% of the total number of S and O constituting the three member rings.
Examples of these compounds include linear organic compounds such as bis(β-epithiopropylthio)methane, 1,2-bis(β-epithiopropylthio)ethane, 1,3-bis(β-epithiopropylthio)propane, 1,2-bis(β-epithiopropylthio)propane, 1-(β-epithiopropylthio)butane, 1,3-bis(β-epithiopropylthio)butane, 1-(β-epithiopropylthio)-3-(β-epithiopropylthiomethyl)butane, 1,5-bis(β-epithiopropylthio)pentane, 1-(β-epithiopropylthio)-4-(β-epithiopropylthio-methyl)pentane, 1,6-bis(β-epithiopropylthio)hexane, 1-(β-epithiopropylthio)-5-(β-epithiopropylthiomethyl)hexane, 1-(β-epithiopropylthio)-2-[(2-(β-epithiopropylthioethyl)thio]ethane and 1-(βepithiopropylthio)-2-[[2-(2-β-epithiopropylthioethyl)thioethyl]thio]ethane; branched organic compounds such as tetrakis(β-epithiopropylthiomethyl)methane, 1,1,1-tris(β-epithiopropylthiomethyl)propane, 1,5-bis(β-epithiopropylthio)-2-(β-epithiopropylthiomethyl)-3-thiapentane, 1,5-bis(β-epithiopropylthio)-2,4-bis(β-epithiopropylthiomethyl)-3-thiapentane, 1-(β-epithiopropylthio)-2,2-bis(β-epithiopropylthiomethyl)-4-thiahexane, 1,5,6-tris(β-epithiopropylthio)-4-(β-epithiopropylthiomethyl)-3-thiahexane, 1,8-bis(β3-epithiopropylthio)-4-(β-epithiopropylthiomethyl)-3,6-dithiaoctane, 1,8-bis(β-epithiopropylthio)-4,5-bis(β-epithiopropylthiomethyl)-3,6-dithiaoctane, 1,8-bis(β-epithiopropylthio)-4,4-bis(β3-epithiopropylthiomethyl)-3,6-dithiaoctane, 1,8-bis(β-epithiopropylthio)-2,4,5-tris(β-epithiopropylthiomethyl)-3,6-dithiaoctane, 1,8-bis(β-epithiopropylthio)-2,5-(β-epithiopropylthiomethyl)-3,6-dithiaoctane, 1,9-bis(β-epithiopropylthio)-5-(β-epithiopropylthiomethyl)-5-[(2-β-epithiopropylthioethylthiomethyl]-3-7-dithianonane, 1,10-bis(β-epithiopropylthio)-5,6-bis[2-β-epithiopropylthioethyl)thio]-3,6,9-trithiadecane, 1,11-bis(β-epithiopropylthio)-4,8-bis(β-epithiopropylthiomethyl)-3,6,9-trithiaundecane, 1,11-bis(β-epithiopropylthio)-5,7-bis(β-epithiopropylthiomethyl)-3,6,9-trithiaundecane, 1,11-bis(β-epithiopropylthio)-5,7-[(2-β-epithiopropylthio)thiomethyl]-3,6,9-trithiaundecane and 1,11-bis(β-epithiopropylthio)-4,7-bis(β-epithiopropylthiomethyl)-3,6,9-trithiaundecane; and compounds obtained by substituting at least one hydrogen atom of the episulfide group in the above compounds with methyl group, cyclic aliphatic organic compounds such as 1,3- and 1,4-bis(β-epithiopropylthio)cyclohexanes, 1,3- and 1,4-bis(β-epithiopropylthiomethyl)cyclohexanes, bis[4-(β-epithiopropylthio)cyclohexyl]methane, 2,2-bis[4-(β-epithiopropylthio)cyclohexyl]propane, bis[4-(β-epithiopropylthio)cyclohexyl]sulfide, 2,5-bis(β-epithiopropylthiomethyl)-1,4-dithiane and 2,5-bis(β-epithiopropylthioethylthiomethyl)-1,4-dithiane; and compounds obtained by subtituting at least one hydrogen atom of the episulfide group in the above compounds with methyl group and aromatic organic compounds such as 1,3- and 1,4-bis(β-epithiopropylthio)benzenes, 1,3- and 1,4-bis(β-epithiopropylthiomethyl)benzenes, bis[4-(β-epithiopropylthio)phenyl]methane, 2,2-bis[4-(β-epithiopropylthio)phenyl]propane, bis[4-(β-epithiopropylthio)phenyl]sulfide, bis[4-(β-epithiopropylthio)phenyl]sulfone and 4,4′-bis(β-epithiopropylthio)biphenyl; and compounds obtained by substituting at least one hydrogen atom of the episulfide group in the above compounds with methyl group. However, compound (a) is not limited to the above compounds shown as examples. The above compounds may be used singly or as a mixture of two or more compounds.
The most preferred episulfide compounds are bis(β-epithiopropyl)sulfide of formula:
##STR00007##
and bis(β-epithiopropyl)disulfide of formula:
##STR00008##
The polymerizable composition of the invention may further include up to 30% by weight, preferably up to 15%, based on the total weight of polymerizable monomers, of one ore more polythiol monomers having two or more, preferably two to four thiol functions.
The polythiol monomers can be represented by formula (VIII):
R′(SH)n′ (VIII)
in which n′ is an integer from 2 to 6, preferably 2 to 4, and R′ is an organic group of valency equal to n′.
Useful polythiol monomers are those disclosed in EP-A-394,495 and U.S. Pat. No. 4,775,733 and the polythiols corresponding to the following formulas:
##STR00009##
and
C2H5C(CH2COOCH2CH2SH)3
Among the preferred polythiol monomers there may be cited aliphatic polythiols such as pentaerythritol tetrakis mercaptoproprionate. 1-(1′-mercaptoethylthio)-2-3-dimercaptopropane, 1-(2′-mercaptopropylthio)-2,3-dimercaptopropane, 1-(3′-mercaptopropylthio)-2,3-dimercaptopropane, 1-(4′-mercaptobutylthio)-2,3-dimercaptopropane, 1-(5′-mercaptopentylthio)-2,3 dimercapto-propane, 1-(6′-mercaptohexylthio)-2,3-dimercaptopropane, 1,2-bis(-4′-mercaptobutylthio)-3-mercaptopropane, 1,2-bis(5′-mercaptopentylthio)-3-mercaptopropane, 1,2-bis(6′-mercaptohexyl)-3-mercaptopropane, 1,2,3-tris(mercaptopropylthio)propane, 1,2,3-tris(3′-mercaptoethylthio)propane, 1,2,3-tris(2′-mercaptoethylthio)propane, 1,2,3-tris(4′-mercaptobutylthio)propane, 1,2,3-tris(6′-mercaptohexylthio)propane, methanedithiol, 1,2-ethanedithiol, 1,1-propanedithiol, 1,2-propanedithiol, 1,3-propanedithiol, 2,2-propanedithiol, 1,6-hexanethiol-1,2,3-propanetrithiol, 1,2-bis(2′-mercaptoethylthio)-3-mercaptopropane, 2-(2-sulfanylethylthio)-3-[3-sulfanyl-2-(2-sulfanylethylthio)propylthio]propane-1-thiol and mixtures thereof.
Preferred polythiol monomers are 1,2-bis(2′-mercaptoethylthio)-3-mercaptopropane and 2-(2-sulfanylethylthio)-3-[3-sulfanyl-2-(2-sulfanylethylthio)propylthio]propane-1-thiol.
The addition of polythiol monomer in the composition of the invention reduces haze and striation and improves smooth polymerization.
The composition of the invention may also include up to 30% by weight, preferably no more than 15%, based on the total weight of polymerizable monomers present in the composition, of one or more polyiso(thio)cyanate, preferably polyisocyanate monomers having two ore more iso(thio)cyanate functions per molecule, preferably two or three iso(thio)cyanate functions.
The preferred polyiso(thio)cyanate monomers are those having the formulae: ##STR00010##
wherein:
R11 is independently H or C1-C5 alkyl group, preferably CH3 or C2H5;
R12 is H, an halogen, preferably Cl or Br, or a C1-C5 alkyl group, preferably CH3 or C2H5;
Z is —N═C═O or —N═C═S, preferably —N═C═O;
a is an integer ranging from 1 to 4, b is an integer ranging from 2 to 4 and a+b≦6; and
x is an integer from 1 to 10, preferably 1 to 6.
Among the preferred polyiso(thio)cyanate monomers there may be cited tolylene diiso(thio)cyanate, phenylene diiso(thio)cyanate, ethylphenylene diiso(thio)cyanate, isopropyl phenylene diiso(thio)cyanate, dimethylphenylene diiso(thio)cyanate, diethylphenylene diiso(thio)cyanate, diisopropylphenylene diiso(thio)cyanate, trimethylbenzyl triiso(thio)cyanate, xylylene diiso(thio)cyanate, benzyl triiso(thio)cyanate, 4,4′-diphenyl methane diiso(thio)cyanate, naphtalene diiso(thio)cyanate, isophorone diiso(thio)cyanate, bis(iso(thio)cyanate methyl)cyclohexane, hexamethylene diiso(thio)cyanate and dicyclohexylmethane diiso(thio)cyanate.
There can be used a single polyiso(thio)cyanate monomer or a mixture thereof.
The addition of the polyiso(thio)cyanate monomer reduces gel time and improves the mechanical performance of the obtained resin.
When both a polythiol monomer and a polyiso(thio)cyanate monomer are present in the composition the weight ratio polyiso(thio)cyanate/polythiol is preferably equal to or less than 1.
The polymerizable compositions according to the invention may also include additives which are conventionally employed in polymerizable compositions intended for moulding optical articles, in particular ophthalmic lenses, in conventional proportions, namely inhibitors, dyes, UV absorbers, perfumes, doedorants, antioxidants, antiyellowing agents and release agents.
The perfumes allow the odour of the compositions to be masked, in particular during surfacing or outering operations.
In particular, usual UV absorbers such as those commercialized under the tradenames UV 5411®, UV 9®, Tinuvin 400® and Tinuvin 312® may be used in amounts generally up to 0.4% by weight of the total polymerizable monomers weight.
Also, the compositions of the invention preferably comprise a release agent in an amount up to 0.1% by weight of the total polymerizable monomers weight.
Among the release agents there may be cited mono and dialkyl phosphates, silicones, fluorinated hydrocarbon, fatty acids and ammoniumm salts. The preferred release agents are mono and dialkyl phosphates and mixtures thereof. Such release agents are disclosed inter alia in documents U.S. Pat. Nos. 4,662,376, 4,975,328 and EP-271.839.
The composition of the present invention can be easily polymerized by mixing the polymerizable monomers with the catalyst system at room temperature or under heat.
Preferably, polymerization is effected by moderate heating and most preferably using a two-step heating process comprising a first step in which the mixture is heated up to gelification at a first temperature of 50° C. or less, preferably at a temperature of 25° C. to 50° C., and thereafter in a second step is heated at a temperature higher than the first temperature, typically up to 90° C. to obtain a hard resin. Preferably, the second temperature ranges from 60 to 90° C. Polymerization process usually lasts for 6 hours or less, typically 3 hours or less. In the case of the two steps heating process, first step typically lasts for about 1 hour and second step lasts for about 2 hours.
In the following examples, unless otherwise stated, all parts and percentages are by weight.
Polymerizable compositions are prepared by mixing at room temperature the components indicated in Table I below. The compositions are poured into the mold cavity of typical two-part glass mould for making optical lenses of optical power −2.00 and −4.25. The compositions are then cured in an oven as indicated in Table I. Properties of the resulting lenses are also given in Table I.
TABLE I
Ex. 1
Ex. 2
C1
C2
Parts by weight
Formulation
Polymerizable monomers
Bis(β-epithio-
100
—
100
100
propyl)disulfide
Bis(β-epithio-
—
100
—
—
propyl)sulfide
Catalytic system
N,N-dimethylcyclohexyl-
—
—
—
0.02
amine
N,N-dicyclohexylmethyl-
0.15
0.15
0.15
0.10
amine
KSCN solution*
0.11
0.11
—
—
Polymerization cycle
Hours
45° C.
1
1
1
1
80° C.
2
2
2
2
State of the composition
Hard resin
Hard resin
No gel
No gel
after polymerization
cycle
Optical lenses having optical powers of −2.00 and −4.25 dioptries are moulded as in examples 1 and 2, using the compositions and polymerization cycle indicated in Table II. Results are also given in Table II.
TABLE II
Ex. 3
C3
C4
Parts by weight
Formulation
Polymerizable monomers
Bis(β-epithiopropyl)sulfide
90.0
90.0
90.0
1,2-bis(2′-mercaptoethylthio)-3-
10.0
10.0
10.0
mercaptopropane
Catalyst system
N,N-dicyclohexylmethylamine
0.15
0.50
—
KSCN solution*
0.11
—
0.29
Polymerization cycle
30° C./1 hour
Gel
No gel
No gel
80° C./2 hours
Hard resin
Much
Runaway
striation
reaction
As shown by example 3, the catalyst system of the invention is very effective to give a fast gel. The use of either a tertiary amine or KSCN solution alone does not give a good fast gel, even with increased catalyst concentration.
Optical lenses having optical powers from −2.00 to −10.00 dioptries are moulded as previously described using the compositions and the polymerization cycles indicated in Table III.
TABLE III
Ex. 4
Ex. 5
Ex. 6
Ex. 7
Ex. 8
Parts by weight
Formulation
Bis(β-
85.0
85.0
90.0
90.0
—
epithiopropyl)disulfide
Bis(β-epithiopropyl)sulfide
—
—
—
—
90.0
Xylylene diisocyanate
7.5
7.5
—
—
—
1,2-bis(2′-mercaptoethyl-
—
7.5
—
10.0
10.0
thio)-3-mercaptopropane
Thiol A***
7.5
—
—
—
—
2-(2-sulfanylethylthio)-3-[3-
—
—
10.0
—
—
sulfanyl-2-(2-sulfanylethyl-
thio)propylthio]propane-1-
thiol**
Catalyst system
Dicyclohexylmethylamine
0.15
0.15
0.15
0.15
0.15
KSCN solution*
0.08
0.08
0.24
0.11
0.11
Polymerization cycle
Hours
45° C.
1
1
1
1
1
80° C.
2
2
2
2
2
State after polymerization
Hard resin
Hard resin
Hard resin
Hard resin
Hard resin
cycle
Lens properties
Striation
No
No
No
No
No
Haze
No
No
No
No
No
Demoulding
No
No
No
No
No
Surface defects
No
No
No
No
No
Softening temperature (° C.)
>80
>80
>80
>80
>80
Yellowness index
1.54
—
—
1.36
—
Tinting (%)
68.0
—
—
74
—
Light transmission (%)
90.0
—
—
90.1
—
nD25
1.73
—
—
1.74
—
Abbe number νD
32
—
—
33
—
*KSCN solution: 8.49% KSCN/34.85% Crown ether (18-crown-6)/56.66% 2-mercaptoethanol
**Mixture of:
##STR00011##
##STR00012##
##STR00013##
***Thiol A is a polythioprepolymer made by reacting xuylylene diisocyanate and 1,2 bis(2′-mercaptoethylthio)-3-mercaptopropane in a molar ratio 1/8.
Optical lenses are made as in the previous examples. Formulation, cure cycle and lens performances are given in the table below.
Parts by weight
Formulation
bis(β-epithiopropyl)disulfide
89.0
XDI
1.0
Polythio prepolymer****
10.0
Dicyclohexylamine
0.60
KSCN solution*
0.10%
Cure cycle
20 C.
20 min (gel)
80 C.
2 hr (post cure)
State after cure cycle
Hard resin
Lens Performance
Striation
No
Haze
No
De-moulding
No
Surface defect
No
Softenning temperature
>80 C.
Yellowness index
1.48
Tinting
71
Light transmission
90.0
Refractive index (nD25)
1.74
Abbe number νD
33
****Polythioprepolymer is a polythiol prepolymer made by mixing and polymerising 2-(2-sulfanylethylthio)-3-[3-sulfanyl-2-(2-sulfanylethyl-thio)propylthio]propane-1-thiol and bis(β-epithiopropyl)disulfide (80/20 weight ratio).
Jiang, Peiqi, Adileh, Fadi O., Turshani, Yassin Yusef
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| 5973098, | Oct 29 1998 | ESSILOR INTERNATIONAL - COMPAGNIE GENERALE D OPTIQUE | Polymerizable compositions for making thio containing resins including a thiocyanate salt catalyst and process for making thio containing resin articles |
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| Executed on | Assignor | Assignee | Conveyance | Frame | Reel | Doc |
| Jun 29 2001 | Essilor International Compagnie General D'Optique | (assignment on the face of the patent) | / | |||
| Sep 21 2001 | JIANG, PEIQI | ESSILOR INTERNATIONAL COMPAGNIE GENERAL D OPTIQUE | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 012458 | /0528 | |
| Sep 21 2001 | TURSHANI, YASSIN YUSEF | ESSILOR INTERNATIONAL COMPAGNIE GENERAL D OPTIQUE | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 012458 | /0528 | |
| Sep 21 2001 | ADILEH, FADI O | ESSILOR INTERNATIONAL COMPAGNIE GENERAL D OPTIQUE | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 012458 | /0528 |
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